1956 - Fellow of the American Association for the Advancement of Science (AAAS)
His scientific interests lie mostly in Biochemistry, Molecular biology, Histone, Gene and Micrococcal nuclease. His Biochemistry study incorporates themes from Biophysics and Mass spectrometry. His Molecular biology research incorporates elements of DNA, Homologous recombination, Protein kinase A, Mutation and Cell cycle.
His Histone octamer and Nucleosome investigations are all subjects of Histone research. His biological study spans a wide range of topics, including Chromatosome, Linker DNA, Histone H1 and Histone code. His work on Proteomics as part of general Gene research is frequently linked to Mycobacterium tuberculosis, bridging the gap between disciplines.
His primary areas of study are Biochemistry, Molecular biology, Histone, DNA and Chromatin. His Biochemistry study integrates concerns from other disciplines, such as Biophysics and Mass spectrometry. His Molecular biology research is multidisciplinary, incorporating perspectives in Histone H2B, Cell culture, Cell biology, Sperm and Cell cycle.
Histone is a component of his Nucleosome, Histone octamer, Histone H1 and Micrococcal nuclease studies. His DNA research is multidisciplinary, relying on both Crystallography, Nuclear magnetic resonance spectroscopy, Two-dimensional nuclear magnetic resonance spectroscopy and Polymerase chain reaction. His Chromatin research incorporates themes from High-mobility group, DNA repair and Circular dichroism.
E. Morton Bradbury mostly deals with Biochemistry, Histone, Proteomics, Gene and Molecular biology. His work on Peptide sequence, Histone octamer and Human proteome project as part of general Biochemistry study is frequently linked to Bottom-up proteomics and Matrix-assisted laser desorption/ionization, bridging the gap between disciplines. E. Morton Bradbury usually deals with Peptide sequence and limits it to topics linked to Cell and Cell culture and Amino acid.
His Histone research is multidisciplinary, incorporating elements of Chromatin, Biophysics and Acetylation. His work carried out in the field of Molecular biology brings together such families of science as Histone methyltransferase, Growth inhibition, Cell growth, Cancer cell and Cell cycle. His research investigates the connection between Histone methyltransferase and topics such as Histone methylation that intersect with issues in Histone H1.
The scientist’s investigation covers issues in Gene, Mycobacterium tuberculosis, Proteomics, Biochemistry and Cell envelope. His Epigenetics, Histone, Polyadenylation and Gene expression study in the realm of Gene interacts with subjects such as Interrupted gene. Mycobacterium tuberculosis is connected with Proteome, Cytoplasm, Genome, Lipid biosynthesis and Cytosol in his research.
The study of Proteomics is intertwined with the study of Cell biology in a number of ways. His is involved in several facets of Biochemistry study, as is seen by his studies on Histone H3, Histone octamer, Histone code, Histone H2A and Histone H1. His Cell envelope research spans across into areas like Peptide sequence, Proteomic Profiling and Cell membrane.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Reversible histone modifications and the chromosome cell cycle.
E. Morton Bradbury;E. Morton Bradbury.
BioEssays (1992)
Histone acetylation reduces nucleosome core particle linking number change
Vicki G. Norton;Brian S. Imai;Peter Yau;E.Morton Bradbury.
Cell (1989)
DNA looping by Ku and the DNA-dependent protein kinase
Robert B. Cary;Scott R. Peterson;Jinting Wang;David G. Bear.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Mobility of positioned nucleosomes on 5 S rDNA
Sari Pennings;Geert Meersseman;E.Morton Bradbury;E.Morton Bradbury.
Journal of Molecular Biology (1991)
Mycobacterium tuberculosis Functional Network Analysis by Global Subcellular Protein Profiling
Kwasi G. Mawuenyega;Christian V. Forst;Karen M. Dobos;John T. Belisle.
Molecular Biology of the Cell (2004)
The FT210 cell line is a mouse G2 phase mutant with a temperature-sensitive CDC2 gene product.
John P.H. Th'ng;Paul S. Wright;Joyce Hamaguchl;Melanie G. Lee.
Cell (1990)
Amino acid residue specific stable isotope labeling for quantitative proteomics
Haining Zhu;Songqin Pan;Sheng Gu;E. Morton Bradbury;E. Morton Bradbury.
Rapid Communications in Mass Spectrometry (2002)
Comprehensive Proteomic Profiling of the Membrane Constituents of a Mycobacterium tuberculosis Strain
Sheng Gu;Jin Chen;Karen M. Dobos;E. Morton Bradbury;E. Morton Bradbury.
Molecular & Cellular Proteomics (2003)
Histone Acetylation and Deacetylation Identification of Acetylation and Methylation Sites of HeLa Histone H4 by Mass Spectrometry
Kangling Zhang;Kangling Zhang;Katherine E. Williams;Lan Huang;Peter Yau.
Molecular & Cellular Proteomics (2002)
Chromatin structure of telomere domain in human sperm.
Irina A. Zalenskaya;E.Morton Bradbury;E.Morton Bradbury;Andrei O. Zalensky.
Biochemical and Biophysical Research Communications (2000)
University of North Carolina at Chapel Hill
University of California, Irvine
University of Kentucky
Chinese University of Hong Kong
University of Calgary
Shal Technologies (United States)
Los Alamos National Laboratory
Institute of Cancer Research
Colorado State University
University of California, Davis
Profile was last updated on December 6th, 2021.
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